Program Overview
This program on Good Documentation Practices (GDP) and Technical Writing Skills is designed to equip mid-senior professionals in the pharmaceutical industry with the knowledge and skills needed to create accurate, compliant, and effective documentation. Delivered by an industry expert with over 25 years of experience, the program emphasizes practical learning through real-life examples, case studies, and hands-on activities. Participants will gain insights into best practices for pharmaceutical documentation, writing for regulatory compliance, and creating user-friendly technical documents, ultimately enhancing operational efficiency and ensuring adherence to industry standards.
Features
- Master the art of writing clear, concise, and compliant technical documents tailored for internal and external stakeholders.
- Learn practical techniques to ensure accuracy, traceability, and consistency in documentation through real-world examples.
- Gain skills in reviewing and editing documents to meet regulatory and operational standards effectively.
Target audiences
- Quality Assurance (QA) Professionals
- Regulatory Affairs Specialists
- R&D Scientists and Technicians
- Manufacturing Supervisors
Curriculum
- 6 Sections
- 18 Lessons
- 1 Day
Expand all sectionsCollapse all sections
- Foundations of Good Documentation Practices (GDP)3
- Regulatory Requirements and Compliance3
- Effective Technical Writing Skills3
- Practical Applications and Tools3
- Document Review and Quality Control3
- Sustaining a Documentation Culture3
Instructor
